Regan R F, Panter S S
Blood Research Division, Letterman Army Institute of Research, Presidio of San Francisco, CA 94129.
Neurosci Lett. 1993 Apr 30;153(2):219-22. doi: 10.1016/0304-3940(93)90326-g.
Hemoglobin (Hb) has been demonstrated to be neurotoxic when injected into the cerebral cortex in vivo. However, associated systemic factors such as ischemia and epileptogenesis have limited investigations of Hb toxicity in the intact central nervous system (CNS). In this study, the neurotoxicity of human Hb was assessed in mixed neuronal and glial neocortical cell cultures derived from fetal mice. Exposure of cultures to Hb for 24-28 h produced widespread and concentration-dependent neuronal death (EC50 1-2.5 microM), without injuring glia. Brief exposures (1-2 h) were not toxic. Neuronal death was completely blocked by the 21-aminosteroid U74500A, the antioxidant Trolox, and the ferric iron chelator deferoxamine. The results of these experiments suggest that, in this system, Hb is a potent neurotoxin, and that Hb neurotoxicity may contribute to secondary injury processes after trauma and intracranial hemorrhage.
血红蛋白(Hb)在体内注入大脑皮层时已被证明具有神经毒性。然而,诸如缺血和癫痫发生等相关全身因素限制了在完整中枢神经系统(CNS)中对Hb毒性的研究。在本研究中,在源自胎鼠的混合神经元和神经胶质新皮层细胞培养物中评估了人Hb的神经毒性。将培养物暴露于Hb 24 - 28小时会导致广泛的、浓度依赖性的神经元死亡(半数有效浓度为1 - 2.5微摩尔),而不会损伤神经胶质细胞。短暂暴露(1 - 2小时)无毒。神经元死亡被21 - 氨基类固醇U74500A、抗氧化剂Trolox和铁螯合剂去铁胺完全阻断。这些实验结果表明,在该系统中,Hb是一种强效神经毒素,并且Hb神经毒性可能导致创伤和颅内出血后的继发性损伤过程。